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取代噻吩酚的急性毒性和正辛醇/水分配系数:测定与 QSAR 分析。

Acute toxicity and n-octanol/water partition coefficients of substituted thiophenols: determination and QSAR analysis.

机构信息

State Key Laboratory of Pollution Control and Resources Reuse, School of the Environment, Nanjing University, Nanjing 210093, PR China.

出版信息

Ecotoxicol Environ Saf. 2012 Apr;78:134-41. doi: 10.1016/j.ecoenv.2011.11.024. Epub 2011 Dec 9.

Abstract

The acute toxicity (-log EC(50)) to Photobacterium phosphoreum and the n-octanol/water partition coefficient (log K(ow)) of 31 kinds of substituted thiophenols were determined at 298.15K. The -log EC(50) values of studied chemicals are between 4.26 and 5.89. Their log K(ow) values are between 1.34 and 4.02. Comparative molecular field (CoMFA) and comparative molecular similarity index analysis (CoMSIA) models established were successful in predicting -log EC(50) and log K(ow) values of halogenated, methylic, amino and methoxy thiophenols. The size of molecule is the main factor influencing the properties. No correlation was found between the properties and their structural and thermodynamic descriptors from DFT calculation.

摘要

在 298.15K 下,测定了 31 种取代噻吩的对发光菌的急性毒性(-log EC(50))和正辛醇/水分配系数(log K(ow))。研究化学品的-log EC(50)值在 4.26 到 5.89 之间。它们的 log K(ow)值在 1.34 到 4.02 之间。建立的比较分子场(CoMFA)和比较分子相似性指数分析(CoMSIA)模型成功地预测了卤代、甲基、氨基和甲氧基噻吩的-log EC(50)和 log K(ow)值。分子大小是影响性质的主要因素。从 DFT 计算中得到的结构和热力学描述符与性质之间没有相关性。

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